M = In born error of metabolism |
Mucopolysaccharidoses
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![mpsa.jpg (12336 bytes)](mpsa.jpg)
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![mpsb.jpg (11780 bytes)](mpsb.jpg)
![mps2.jpg (19543 bytes)](mps2.jpg)
![mps5.jpg (17527 bytes)](mps5.jpg)
m50 =
Hydroxykynureninuria
autosomal
recessive
m51 = Hydroxyprolinemia
autosomal
recessive
M52 = Hyperlipidemia(Broad beta
disease type III)
autosomal dominant
m53 = Hyperlysinemia
autosomal recessive
m54 =
Hyperornithinemia(Hyperammonemia)
m55 = Hyperoxaluria
autosomal recessive
m56 = Hyperprolinemia type I
autosomal recessive
m57 = Hyperprolinemia type II
autosomal recessive
m58 = Hyperuric aciduria(Lesch-Nyhan syndrome)
X-linked recessive
M59 = Hyperuricemia
autosomal dominant
m60 = Hypervalinemia
autosomal recessive
m61 = Hypophosphatasia
autosomal recessive
m62 = Idiopathic spontaneous hypoglycemia
autosomal recessive
m63 = Infantile amaurotic idiocy(GM2
gangliosidosis,Tay-Sachs disease)
autosomal recessive
m64 = Infantile cerebroside
lipidosis (Gaucher's disease)
autosomal recessive
m65 = Isovaleric acidemia
autosomal recessive
m66 = Juvenile cerebral atrophy
autosomal
recessive
( Juvenile amaurotic idiocy,Vogt-Spielmeyer
disease )
m67 = Juvenile GM2 gangliosidosis
autosomal recessive
m68 = Late infantile GM1 gangliosidosis
m69 = Lipochondrodystrophy(Gargoylism)
autosomal recessive
M70 = Malignant Hyperthermia
autosomal dominant
m71 = Maple
syrup urine disease
autosomal recessive
m72 = Methyl beta hydroxybutyric aciduria
m73 = Methyl crotonyl glycinuria autosomal
recessive
m74 = Methyl malonic aciduria(Propionate
metabolism)
autosomal recessive
m75 = Monosaccharide malabsorption
autosomal recessive
m76 = Mucopolysaccharidosis type IH
( Hurler 's disease)
autosomal recessive
m77 = Mucopolysaccharidosis type IS
( Scheie 's disease)
autosomal recessive
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Dr.Jarind B. Sriraumpuch |
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Update since
10/09/50